GB951065A - Resinous condensation products and laminates prepared therewith - Google Patents

Resinous condensation products and laminates prepared therewith

Info

Publication number
GB951065A
GB951065A GB21165/60A GB2116560A GB951065A GB 951065 A GB951065 A GB 951065A GB 21165/60 A GB21165/60 A GB 21165/60A GB 2116560 A GB2116560 A GB 2116560A GB 951065 A GB951065 A GB 951065A
Authority
GB
United Kingdom
Prior art keywords
phenol
atoms
under reduced
reduced pressure
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB21165/60A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB951065A publication Critical patent/GB951065A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/42Block-or graft-polymers containing polysiloxane sequences
    • C08G77/46Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G8/00Condensation polymers of aldehydes or ketones with phenols only
    • C08G8/28Chemically modified polycondensates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Reinforced Plastic Materials (AREA)
  • Epoxy Resins (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

A co-condensate is made by heating a substantially anhydrous mixture comprising, by weight, 50-96% of a phenol-formaldehyde resole, 30-2% of a silane or siloxane having one of the formulae: <FORM:0951065/C3/1> and <FORM:0951065/C3/2> wherein R is an alkyl group having 1 to 4 C atoms, R1 is an aryl radical and each R2 is an alkyl or alkoxy radical of 1 to 4 C atoms or an aryl radical, and n is 0, 1 or 2, and 20-2% of glycidyl polyether having an epoxide equivalent of at least 170, the epoxy resin being introduced initially or after reaction of the other materials, and removing the liberated alkanol. The reaction may be effected by heating the reactants to reflux temperature and removing the alkanol formed, but is preferably effected under reduced pressure. When making the co-condensate it is preferred to add a little polycarboxylic acid or anhydride, e.g. mellitic, chlorendic, phthalic, terephthalic and adipic acids or anhydrides, the dianhydride of pyromellitic acid being preferred. The products are preferably diluted to 40-70% (wt.) of resin solids with an anhydrous low-boiling acyclic mono- or poly-hydric alcohol of 1-4 C atoms, e.g. ethanol, n-propanol, isopropanol or ethylene glycol. The resoles and organosilicon reactants used are well known, and the epoxy resins used are those obtained by reacting epichlorohydrin with a phenol or a polyhydric alcohol, e.g. as described in U.S.A. Specification 2,640,037. In a typical example (1), a glycidyl polyether of bisphenol A is added to the reaction product of phenol, paraformaldehyde and hexamethylenetetramine and the mixture is heated under reduced pressure; phenyltrimethoxysilane is then added and the mixture is again heated under reduced pressure with removal of methanol by distillation, cooled and mixed with isopropanol to provide a solution containing 60% (wt.) of resin solids.
GB21165/60A 1959-06-18 1960-06-16 Resinous condensation products and laminates prepared therewith Expired GB951065A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US821095A US3074904A (en) 1959-06-18 1959-06-18 Laminate structures

Publications (1)

Publication Number Publication Date
GB951065A true GB951065A (en) 1964-03-04

Family

ID=25232487

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21165/60A Expired GB951065A (en) 1959-06-18 1960-06-16 Resinous condensation products and laminates prepared therewith

Country Status (2)

Country Link
US (1) US3074904A (en)
GB (1) GB951065A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5015529A (en) * 1986-12-24 1991-05-14 Occidental Chemical Corporation Phenolic molding compositions
US5066693A (en) * 1988-09-14 1991-11-19 Occidental Chemical Corporation Molding compositions of resole phenolic resin and epoxy resin
EP1086972A1 (en) * 1999-01-29 2001-03-28 Arakawa Chemical Industries, Ltd. Hardener for epoxy resin, epoxy resin composition, and process for producing silane-modified phenolic resin
DE102008055042A1 (en) 2008-12-19 2010-06-24 Hüttenes-Albertus Chemische Werke GmbH Modified phenolic resins

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL125741C (en) * 1963-05-10 1900-01-01
US3755223A (en) * 1969-12-05 1973-08-28 Dyna Therm Corp An epoxy ablative coating containing a silicone resin, a fibrous reinforcing material, and a non-alkali metal phosphate and borate salt mixture
US5736619A (en) * 1995-04-21 1998-04-07 Ameron International Corporation Phenolic resin compositions with improved impact resistance
US6875807B2 (en) 2003-05-28 2005-04-05 Indspec Chemical Corporation Silane-modified phenolic resins and applications thereof
SE543346C2 (en) * 2018-04-20 2020-12-08 Stora Enso Oyj Process for preparing a bonding resin comprising lignin, phenol and formaldehyde

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2687396A (en) * 1952-07-14 1954-08-24 Dow Corning Composition of silicon-alkyd resin, an epoxy resin, and a phenol-formaldehyde resin
US2810676A (en) * 1956-04-02 1957-10-22 Dow Chemical Co Anthelmintic solutions comprising piperazine compounds

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5015529A (en) * 1986-12-24 1991-05-14 Occidental Chemical Corporation Phenolic molding compositions
US5066693A (en) * 1988-09-14 1991-11-19 Occidental Chemical Corporation Molding compositions of resole phenolic resin and epoxy resin
EP1086972A1 (en) * 1999-01-29 2001-03-28 Arakawa Chemical Industries, Ltd. Hardener for epoxy resin, epoxy resin composition, and process for producing silane-modified phenolic resin
EP1086972A4 (en) * 1999-01-29 2001-07-11 Arakawa Chem Ind Hardener for epoxy resin, epoxy resin composition, and process for producing silane-modified phenolic resin
US6441106B1 (en) 1999-01-29 2002-08-27 Arakawa Chemical Industries, Ltd. Hardener for epoxy resin, epoxy resin composition, and process for producing silane-modified phenolic resin
DE102008055042A1 (en) 2008-12-19 2010-06-24 Hüttenes-Albertus Chemische Werke GmbH Modified phenolic resins
US8563662B2 (en) 2008-12-19 2013-10-22 Huttenes-Albertus Chemische Werke Gmbh Modified phenolic resins
US8569425B2 (en) 2008-12-19 2013-10-29 Huttenes-Albertus Chemische Werke Gmbh Modified phenolic resins

Also Published As

Publication number Publication date
US3074904A (en) 1963-01-22

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